FIELD OF THE INVENTIONThe invention relates to an appliance for material separation (sealing) of the surface of a bone cavity, which is exposed during apicoectomy above the root apex of a root of a tooth, from the resection area on the root of the tooth and from the exposed root canal and a root cavity produced at the end of the canal for closing it on the side of the bone cavity, in particular during an irrigation and filling of the root canal and of the root cavity.
BACKGROUND OF THE INVENTIONThe process for such an apicoectomy is described in detail by Kirschnet, "Atlas der chirurgischen Zahnerhaltung", Munich/Vienna 1987, page 130 to page 135. It entails, after the mucoperiosteum has been lifted, removing as much bone substance from the vicinity of the root apex to be resected as is necessary for performing the operation. The resulting bone cavity has a characteristic spatial shape corresponding to the root apex. After about 20% of the total length of the root has been resected, in most cases a retrograde root canal cavity is produced, and this must be filled just like the root canal itself. In this case, it is possible to insert a pin into the root canal so that only a little filling material is used.
Intraoperative root fillings require that the root canal be irrigated with highly reactive reagents such as 3% strength H2 O2, 5% strength NaOCl, alcohol, etc. These irrigations emerge at the area of resection and are aspirated there, but it is not possible to avoid having a portion of the irrigations enter the bone cavity. In the case of retrograde filling, which is sometimes needed, it is also necessary to prepare the root cavity with highly reactive reagents, for example 40% strength citric acid. In this case as well, it is often unavoidable that liquid enters the bone cavity. On the other hand, the fillings have to be introduced into a dry root cavity or a completely dry root canal, and must be able to harden for a considerable time without liquid entering. Since the fillings must be introduced in excess, it is also often unavoidable that, because of the consistency of these fillings, a portion thereof enters the bone cavity and must be laboriously removed therefrom.
Oozing blood emerges from the surface adjoining the bone cavity and prevents drying both of the root cavity and of the root canal before introduction of the fillings, and contaminates the filling materials in their hardening phase.
For it to be possible, nevertheless, to carry out a satisfactory apicoectomy, it is necessary either to pack the root cavity tightly with gauze, to administer reagents which stop the bleeding due to a vasoconstrictor or astringent action, or to line the bone cavity with bone wax. In this case, it is not advantageous to administer epinephrine or the like, because of the long exposure time, the uncertain onset of its action, the uncertain duration of its action, and its hazardous side effects, especially since renewed bleeding may occur at each irrigation of the bone cavity between times. Although covering the bone surface with the aid of bone wax, which must be carried out with the bone cavity as dry as possible (after administration of hemostatic reagents), prevents further emergence of blood, it has the disadvantage that the wax particles must be removed again after the operation, which requires troublesome manipulation.
In order to eliminate these deficiencies, it has already been disclosed by Wilstermann, "Der retrograde Wurzelkanalverschluβ mit Goldent", Deutsche Zahnarztliche Zeitschrift 29 (1974), pages 759 to 760, to place over the exposed root cross-section the ring-shaped loop of a ring-shaped instrument provided with a handle, which loop separates the area of resection from the surrounding retrogradely prepared bone cavity to such an extent that the root cavity and the root canal remain dry. In this case, however, a viewing restriction for the surgeon is unavoidable, and access to the area of resection is also restricted. In addition, this ring-shaped instrument has to be held throughout the treatment time. Obviously, however, this considerably impedes the work for the surgeon.
An object of the invention is therefore to provide an appliance of the type mentioned above, which remains in situ throughout the operation without having to be held, which allows clear viewing and free access to the resected area of the root apex and to the root cavity or the root canal, which can be produced easily and at low cost, and which can be introduced into the bone cavity and can be adapted in a simple manner to the particular spatial shape thereof.
SUMMARY OF THE INVENTIONThis object is achieved according to the invention by the appliance being a relatively thin-wall lining which almost completely covers the surface of the bone cavity, the lining being capable of easy plastic deformation and being adaptable with the application of minimal force to the spatial shape of the surface but, on the other hand, having a residual elasticity of a magnitude sufficient to retain it in the bone cavity with a small initial tension, the lining having on its side facing the surface of the bone cavity a hemostatic and/or liquid-absorbent material.
The appliance according to the invention achieves in a surprisingly simple manner the object which has been outlined. A lining of this type can conveniently be adapted to all spatial shapes which can occur, either by various punches having respective shapes, by an elastic intermediate layer, or by manual shaping outside the bone cavity, especially when the latter is very large and the use of a punch is inconvenient. The punch is advantageously designed with thin walls, so that the root canal is easily visible on introduction of the lining into the bone cavity. Complete material separation of the surrounding bone material from the root of the tooth is now ensured, it being possible for the lining to be inserted into the bone cavity as soon as the latter is produced, and to remain therein without problems until the root filling is hardened and the operation is complete. It does not hinder the manipulations which are required, nor interfere with visual inspection thereof. The layers can without a problem have compositions which ensure that no particles can be torn out and remain in the bone cavity. The blood which emerges in the region between the lining and the bone tissue and which also coagulates there contributes to improving the adhesion of the lining. The lining itself can be produced in large numbers at very low cost, especially as a flat-web blank, and can be processed on site to an appropriate fit using scissors or the like. Emergence of blood is reliably prevented, even in the region of the bone area adjoining the area of resection, when the slightly plastic, hemostatic and/or liquid-absorbing layer is drawn over the edges of the layer responsible for the shape, so that the corner spaces are also sealed.
BRIEF DESCRIPTION OF THE DRAWINGSThe invention is explained in detail hereinafter by means of an exemplary embodiment shown in the drawings, in which:
FIG. 1, 1a is a diagrammatic fragmentary perspective view showing a root apex of a root of a tooth which has been exposed and resected through an artificially produced bone cavity, and showing an appliance according to the invention which is inserted in this region;
FIG. 2 is a top view of the subject matter of FIG. 1;
FIG. 3 is a sectional view taken along theline 3--3 in FIG. 2;
FIG. 4 is a sectional view taken along theline 4--4 in FIG. 2;
FIG. 5 is a view similar to FIG. 2 but before introduction of the appliance according to the invention;
FIG. 6 is a view similar to FIG. 5, but depicting the introduction of the appliance; and
FIG. 7 is a view similar to FIG. 4 but showing an alternative embodiment of the appliance according to the invention.
DETAILED DESCRIPTIONFIG. 1 is a diagrammatic view showing the area of a jawbone in the region of a resected root apex. In this case, the adjoining mucoperiosteal flap has been cut away from thebone 1 to such an extent that the region of operation is exposed. The lifted flap itself is omitted from the drawing, but therelevant incision site 2 is evident. Abone cavity 3 has been produced in thebone 1, and itscut surface 4 is evident in FIG. 1. The shape of thebone cavity 3 is clear, in particular, from FIGS. 2 to 4. The apicoectomy has already been performed in FIG. 1, so that aresection area 5 is visible. A root cavity 7, which is produced in the dentine of the root 6 of the tooth, is provided for retrograde filling. The root canal 8 is, in FIG. 1, already filled with aroot filling material 9. Alining 10 according to the invention, which is composed of anouter layer 11 and aninner layer 12, is located in thebone cavity 3. In the top view in FIG. 2, and in the enlarged sectional views of FIGS. 3 and 4, which are rotated by 90° , the details of the lining are even more evident. Moreover, in FIG. 4 it can also be seen that thelayer 11 nearest the bone has its edges curling around theedges 12a of thesecond layer 12 which faces the cavity. According to the invention,layer 11 is very easily plasticized, as a result of which satisfactory sealing between thebone cavity 3 and thesurface 4 of thebone 1 takes place, especially in the region of theresection area 5. Blood 13, which emerges at the regions of thesurface 4 not directly covered by thelayer 11, coagulates (FIGS. 3 and 4) and ensures that no further blood can emerge from the incisedbone 1 and interfere with the continuation of the operation.
FIGS. 5 and 6 show, in a highly simplified form, how thelining 10 in a blank or flat form can be pushed manually with the aid of a tamper 14 into thebone cavity 3, during which thelining 10 is reshaped into the final shape conforming to the cavity. The tamper 14 has, apart from ahandle 15, apunch 16 which forms the actual tool for reshaping theblank lining 10. As evident from FIG. 5, thepunch 16 undergoes positive connection to thelining 10, in this case through engagement of arecess 17 in thepunch 16 with apeg 18 provided on thelining 10 on the side thereof having thelayer 12. Positive connection between thelining 10 or itslayer 12 and thepunch 16 can be effected in a variety of ways, another example of which is shown in FIG. 7. In FIG. 7, several pairs ofcooperating recesses 17 andpegs 18 are provided. Instead of this, it is also possible to use strips, or annular positive connections.
In place of the deformation (FIGS. 5 to 7) of thelining 10 with the aid of a tamper 14 orpunch 16, it is also possible, especially when thebone cavity 3 is very large and, for example, embraces the region of the roots 6 of several teeth, to manually shape alining 10 of this type outside the mouth so that it is approximately adapted to the bone cavity. After making any corrections which are necessary, thelining 10 can be used in this form in a manner appropriate for the function.
Thelayer 11 should undergo plastic deformation very easily, and should be hemostatic and/or liquid-absorbent, especially on itsside 19 facing thesurface 4 of thebone cavity 3. It is expediently composed of regenerated, oxidized cellulose or natural bovine collagen or thrombin. On the other hand, an appropriate metallic material or plastic which is, where appropriate, chosen to be hardenable, is used for thelayer 12. It is essential that thislayer 12 retains, after its deformation, a residual elasticity of a magnitude sufficient for the lining 10 to be held fast in thebone cavity 3 with an initial tension which, although slight, is sufficient that the surgeon can "forget" about the lining after its positioning by the surgeon. The twolayers 11 and 12 are firmly connected together, for example by bonding with fibrin.
It is also possible to provide, between thelayers 11 and 12, anintermediate layer 20 which is composed of an elastic plastic material and is designed to be sufficiently thick that the relativelythin layer 11 adapts better to thesurface 4 and, where appropriate, compensates for roughness present there. It is, of course, necessary for all materials used to be sterilizable. It has been found that a thickness of 0.5 to 1.0 mm is optimal for the lining 10 for the purpose of application.
Although particular preferred embodiments of the invention has been disclosed in detail for illustrative purposes, it will be recognized that variations or modifications of the disclosed apparatus, including the rearrangement of parts, lie within the scope of the present invention.